Severity: Warning
Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Aza-dipyrromethenes are ligands for a number of useful fluorescent dyes and electronic materials. They have high absorption in the red and NIR range. Fused-ring aza-dipyrromethenes cannot be synthesized through the same methods used to make aza-dipyrromethenes, which are common commercial dyes. The current synthesis is limited to treating a phthalonitrile-based electrophile with a Grignard reagent followed by reduction with formamide at high temperature. In this work, we introduce a new fused-ring aza-dipyrromethene synthesis from ortho-lithiated aromatic nitriles. This method allows for a much wider range of functional groups, less complicated starting materials, and yields that are consistent with the highest reported for aza-dipyrromethenes of any kind.
Download full-text PDF |
Source |
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http://dx.doi.org/10.1039/c8cc04658a | DOI Listing |
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